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Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy
The aim was to examine whether clinical seizures and amplitude-integrated electroencephalogram (aEEG) patterns in infants with hypoxic ischemic encephalopathy (HIE) can predict the extent of brain injury on magnetic resonance images (MRI) and the long-term neurodevelopmental outcomes at 18∼24 months...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282004/ https://www.ncbi.nlm.nih.gov/pubmed/33761675 http://dx.doi.org/10.1097/MD.0000000000025118 |
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author | Lin, Yen-Kuang Hwang-Bo, Seok Seo, Yu-Mi Youn, Young-Ah |
author_facet | Lin, Yen-Kuang Hwang-Bo, Seok Seo, Yu-Mi Youn, Young-Ah |
author_sort | Lin, Yen-Kuang |
collection | PubMed |
description | The aim was to examine whether clinical seizures and amplitude-integrated electroencephalogram (aEEG) patterns in infants with hypoxic ischemic encephalopathy (HIE) can predict the extent of brain injury on magnetic resonance images (MRI) and the long-term neurodevelopmental outcomes at 18∼24 months of age. HIE infants who underwent therapeutic hypothermia (TH) between June 2014 and March 2017 were included in this study. Infants with clinical seizure were analyzed for aEEG patterns and the extent of brain injury on MRI findings. Clinical seizure, aEEG, and brain MRI were assessed and compared with neurodevelopmental outcomes at 18∼24 months of age. Among the 97 HIE infants enrolled in this study with brain MRI scans, 78 (73.1%) TH-treated HIE infants exhibited clinical seizures. More abnormalities on a EEGs and more significant use of first and second antiepileptic drugs (AEDs) were significantly higher in the clinical-seizure group with longer hospitalized days. At a corrected 18 to 24 months of age, HIE infants in the clinical-seizure group with more extension of injury lesions on diffusion-weighted MRI scans exhibited significantly more delayed neurodevelopment. A risk factor analysis indicated that male infants who stayed in the hospital for more than 11 days were at a higher risk of having clinical seizures. The lesion size in MRI greater than 37 pixels was a risk factor with an 81.8% accuracy. Seizures in HIE infants may predict abnormal brain MRI scans and abnormal neurodevelopment at 18 to 24 months of age. |
format | Online Article Text |
id | pubmed-9282004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-92820042022-08-02 Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy Lin, Yen-Kuang Hwang-Bo, Seok Seo, Yu-Mi Youn, Young-Ah Medicine (Baltimore) 6200 The aim was to examine whether clinical seizures and amplitude-integrated electroencephalogram (aEEG) patterns in infants with hypoxic ischemic encephalopathy (HIE) can predict the extent of brain injury on magnetic resonance images (MRI) and the long-term neurodevelopmental outcomes at 18∼24 months of age. HIE infants who underwent therapeutic hypothermia (TH) between June 2014 and March 2017 were included in this study. Infants with clinical seizure were analyzed for aEEG patterns and the extent of brain injury on MRI findings. Clinical seizure, aEEG, and brain MRI were assessed and compared with neurodevelopmental outcomes at 18∼24 months of age. Among the 97 HIE infants enrolled in this study with brain MRI scans, 78 (73.1%) TH-treated HIE infants exhibited clinical seizures. More abnormalities on a EEGs and more significant use of first and second antiepileptic drugs (AEDs) were significantly higher in the clinical-seizure group with longer hospitalized days. At a corrected 18 to 24 months of age, HIE infants in the clinical-seizure group with more extension of injury lesions on diffusion-weighted MRI scans exhibited significantly more delayed neurodevelopment. A risk factor analysis indicated that male infants who stayed in the hospital for more than 11 days were at a higher risk of having clinical seizures. The lesion size in MRI greater than 37 pixels was a risk factor with an 81.8% accuracy. Seizures in HIE infants may predict abnormal brain MRI scans and abnormal neurodevelopment at 18 to 24 months of age. Lippincott Williams & Wilkins 2021-03-26 /pmc/articles/PMC9282004/ /pubmed/33761675 http://dx.doi.org/10.1097/MD.0000000000025118 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 6200 Lin, Yen-Kuang Hwang-Bo, Seok Seo, Yu-Mi Youn, Young-Ah Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title | Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title_full | Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title_fullStr | Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title_full_unstemmed | Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title_short | Clinical seizures and unfavorable brain MRI patterns in neonates with hypoxic ischemic encephalopathy |
title_sort | clinical seizures and unfavorable brain mri patterns in neonates with hypoxic ischemic encephalopathy |
topic | 6200 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282004/ https://www.ncbi.nlm.nih.gov/pubmed/33761675 http://dx.doi.org/10.1097/MD.0000000000025118 |
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